Cartilage-disruption factor involved in Kashin-Beck disease
大骨节病涉及的软骨破坏因子
基本信息
- 批准号:08044293
- 负责人:
- 金额:$ 1.73万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for international Scientific Research
- 财政年份:1996
- 资助国家:日本
- 起止时间:1996 至 无数据
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
1 The development of a Kashin-Beck Disease model (monkey) Monkeys were fed with water and food from the Kashin-Beck Disease area, and sera were obtained from these animals.2 sera were obtained from patients with Kashin-Beck Disease.3 Chinese and Japanese investigators discussed studies on Kashin-Beck Disease.4 MMP-9-inducing factors in sera from patients with Kashin-Beck Disease.Rabbit growth plate chondrocytes were incubated for 4 or 8 days in the presence of 5% control sera or 5% sera from patients with Kashin-Beck Disease. Gelatinese activity was estimated by gelatin zymography. No gelatinase activity was found in the cell layr, but MMP-2 were found in the conditioned medium. The sera from patients with Kashin-Beck Disease induced MMP-9 of 92kDa on day 4, and increased MMP-9 levels 3-to 4-fold on day 8 relative to control sera. These findings suggest that sera from patients with Kashin-Beck Disease contain factors that stimulate MMP-9 synthesis by growth plate chondrocytes.
1大骨节病模型(猴)的建立用来自大骨节病区的水和食物喂养猴,3中国和日本研究者讨论了大骨节病的研究。4大骨节病患者血清中MMP-9诱导因子,将兔生长板软骨细胞在5%对照血清或5%大骨节病患者血清存在下孵育4或8天。明胶酶谱法测定明胶酶活性。细胞层中无明胶酶活性,但条件培养液中有MMP-2表达。与对照血清相比,大骨节病患者血清在第4天诱导了92 kDa的MMP-9,并且在第8天使MMP-9水平增加3- 4倍。这些发现表明,大骨节病患者的血清中含有刺激生长板软骨细胞合成MMP-9的因子。
项目成果
期刊论文数量(17)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Hashimoto K.,Noshiro M.,Ohno S.,Kawamoto T.,Satakeda H.,Akagawa Y.,Nakashima K.,Okimura A.,Ishida H.,Okamoto T.,Pan H.,Shen M.,Yan W.,Kato Y.: "Characterization of a cartilage-derived 66kDa protein (RGD-CAP/big-h3) that Binds to collagen" Biochem.Biophys.
桥本 K.、能代 M.、大野 S.、川本 T.、佐武田 H.、赤川 Y.、中岛 K.、冲村 A.、石田 H.、冈本 T.、潘 H.、沉明、严伟
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- 影响因子:0
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Jikko A.,Hiranuma H.,Iawamoto M.,Kato Y.,Okada Y.,Fuchihata H.: "Effects of X irradiation on metabolism of proteoglycans" Radiation Res.146. 93-99 (1996)
Jikko A.、Hiranuma H.、Iawamoto M.、Kato Y.、Okada Y.、Fuchihata H.:“X 辐射对蛋白聚糖代谢的影响”辐射 Res.146。
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- 影响因子:0
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Nakamura S.,Kamihagi K.,Satakeda H.,Katayama M.,Pan H.,Okamoto H.,Noshiro M.,Takahashi K.,Yoshihara Y.,Shimmei M.,Okada Y and Kato Y.: "Enhancement of SPARC/osteonectin synthesis in arthritic cartilage : its increased levels in Synovial Fluids from Patien
Nakamura S.、Kamihagi K.、Satakeda H.、Katayama M.、Pan H.、Okamoto H.、Noshiro M.、Takahashi K.、Yoshihara Y.、Shimmei M.、Okada Y 和 Kato Y.:“增强
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Okimura A., Makihira S., and Kato Y.: "Cartilage-matrix protein synthesis is enhanced in arthritic cartilage." Arthritis Rheum. (in press).
Okimura A.、Makihira S. 和 Kato Y.:“关节炎软骨中软骨基质蛋白合成得到增强。”
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- 影响因子:0
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Hashimoto K., Noshiro M., Ohno S., Kawamoto T., Satakeda H., Akagawa Y., Nakashima K., Okimura A., Ishida H., Okamoto T., Pan H., shen M., Yan W., Kato Y.: "Characterization of a cartilage-derived 66kDa protein (RGD-CAP/big-h3) that betainds to collagen"
桥本 K.、Noshiro M.、Ohno S.、川本 T.、佐竹田 H.、赤川 Y.、中岛 K.、冲村 A.、石田 H.、冈本 T.、潘 H.、沉 M.、严 W
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KATO Yukio其他文献
AMP-activated protein kinase activation reduces the transcriptional activity of the murine luteinizing hormone β-subunit gene
AMP 激活的蛋白激酶激活降低了小鼠黄体生成素 β 亚基基因的转录活性
- DOI:
10.1262/jrd.2019-143 - 发表时间:
2020 - 期刊:
- 影响因子:1.8
- 作者:
MORIYAMA Ryutaro;IWAMOTO Koichi;HAGIWARA Teruki;YOSHIDA Saishu;KATO Takako;KATO Yukio - 通讯作者:
KATO Yukio
下垂体の機能維持と幹・前駆細胞: Pituitary stem/progenitor cells for pituitary homeostasis
维持垂体功能和干/祖细胞:垂体干/祖细胞用于垂体稳态
- DOI:
- 发表时间:
2018 - 期刊:
- 影响因子:0
- 作者:
YOSHIDA Saishu;FUJIWARA Ken;INOUE Takashi;SASAKI Erika;KAMETANI Yoshie;TAKEKOSHI Susumu;INOSHITA Naoko;KATO Takako;KATO Yukio;吉田彩舟 - 通讯作者:
吉田彩舟
下垂体組織幹・前駆細胞の特性とその起源の多様: Characteristics and plural origins of stem/progenitor cells in the pituitary gland
垂体干细胞/祖细胞的特征和多重起源
- DOI:
- 发表时间:
2018 - 期刊:
- 影响因子:0
- 作者:
YOSHIDA Saishu;FUJIWARA Ken;INOUE Takashi;SASAKI Erika;KAMETANI Yoshie;TAKEKOSHI Susumu;INOSHITA Naoko;KATO Takako;KATO Yukio;吉田彩舟;吉田彩舟 - 通讯作者:
吉田彩舟
KATO Yukio的其他文献
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{{ truncateString('KATO Yukio', 18)}}的其他基金
Transdermal drug delivery targeted to xenobiotics ABC transporters expressed in the skin
针对皮肤中表达的异生素 ABC 转运蛋白的透皮给药
- 批准号:
25670011 - 财政年份:2013
- 资助金额:
$ 1.73万 - 项目类别:
Grant-in-Aid for Challenging Exploratory Research
The development of culture surfaces expressing functional groups that enhance isolation, proliferation and differentiation of mesenchymal stem cells.
表达增强间充质干细胞分离、增殖和分化的功能基团的培养表面的开发。
- 批准号:
24659876 - 财政年份:2012
- 资助金额:
$ 1.73万 - 项目类别:
Grant-in-Aid for Challenging Exploratory Research
Development of triple-target antitumor drugs recognized by oligopeptide transporters
寡肽转运蛋白识别的三靶点抗肿瘤药物的开发
- 批准号:
23659019 - 财政年份:2011
- 资助金额:
$ 1.73万 - 项目类别:
Grant-in-Aid for Challenging Exploratory Research
Digital Archives and Early Modern English Theatre: The Network of Playhouses, Players, and Printing-houses
数字档案和早期现代英国戏剧:剧场、演员和印刷厂的网络
- 批准号:
23320059 - 财政年份:2011
- 资助金额:
$ 1.73万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
The molecular mechanism by which transcriptional factor DEC1 modulates circadian rhythms of blood pressure.
转录因子 DEC1 调节血压昼夜节律的分子机制。
- 批准号:
23390423 - 财政年份:2011
- 资助金额:
$ 1.73万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Serum-free medium for dental regenerative tissue engineering
用于牙科再生组织工程的无血清培养基
- 批准号:
23659918 - 财政年份:2011
- 资助金额:
$ 1.73万 - 项目类别:
Grant-in-Aid for Challenging Exploratory Research
Studies of the roles of pituitary transcription factors for pituitary development and progenitor cells
垂体转录因子对垂体发育和祖细胞作用的研究
- 批准号:
21380184 - 财政年份:2009
- 资助金额:
$ 1.73万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Research of transporter-adaptor network as target of drug effect and toxicity
转运蛋白-适配器网络作为药效和毒性靶标的研究
- 批准号:
20390047 - 财政年份:2008
- 资助金额:
$ 1.73万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Studies for mechanisms of gonadotropin gene regulation with novel pituitary transcription factors
新型垂体转录因子促性腺激素基因调控机制研究
- 批准号:
18380177 - 财政年份:2006
- 资助金额:
$ 1.73万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Roles of transporter adaptors as regulatory mechanism for drug absorption and disposition
转运蛋白适配器作为药物吸收和处置调节机制的作用
- 批准号:
18590137 - 财政年份:2006
- 资助金额:
$ 1.73万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
相似国自然基金
抑制肿瘤转移的新靶点: iPLA2在整合素和基质金属蛋白酶再循环中的新颖作用
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- 批准年份:2016
- 资助金额:25.0 万元
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